DK271289A - Fremgangsmaade til fremstilling af hydroxysyrer - Google Patents

Fremgangsmaade til fremstilling af hydroxysyrer Download PDF

Info

Publication number
DK271289A
DK271289A DK271289A DK271289A DK271289A DK 271289 A DK271289 A DK 271289A DK 271289 A DK271289 A DK 271289A DK 271289 A DK271289 A DK 271289A DK 271289 A DK271289 A DK 271289A
Authority
DK
Denmark
Prior art keywords
preparation
phenylbutyric acid
procedure
dehydrogenase
hydroxy acids
Prior art date
Application number
DK271289A
Other languages
English (en)
Other versions
DK172667B1 (da
DK271289D0 (da
Inventor
Oreste Ghisalba
Daniel Gygax
Rene Lattmann
Hans-Peter Schaer
Elke Schmidt
Gottfried Sedelmeier
Original Assignee
Ciba Geigy Ag
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Ciba Geigy Ag filed Critical Ciba Geigy Ag
Publication of DK271289D0 publication Critical patent/DK271289D0/da
Publication of DK271289A publication Critical patent/DK271289A/da
Application granted granted Critical
Publication of DK172667B1 publication Critical patent/DK172667B1/da

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12PFERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P7/00Preparation of oxygen-containing organic compounds
    • C12P7/40Preparation of oxygen-containing organic compounds containing a carboxyl group including Peroxycarboxylic acids
    • C12P7/52Propionic acid; Butyric acids
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12PFERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P7/00Preparation of oxygen-containing organic compounds
    • C12P7/40Preparation of oxygen-containing organic compounds containing a carboxyl group including Peroxycarboxylic acids
    • C12P7/42Hydroxy-carboxylic acids
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/347Preparation of carboxylic acids or their salts, halides or anhydrides by reactions not involving formation of carboxyl groups
    • C07C51/367Preparation of carboxylic acids or their salts, halides or anhydrides by reactions not involving formation of carboxyl groups by introduction of functional groups containing oxygen only in singly bound form
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K5/00Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/06Dipeptides
    • C07K5/06139Dipeptides with the first amino acid being heterocyclic

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Biochemistry (AREA)
  • Genetics & Genomics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Health & Medical Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Microbiology (AREA)
  • General Engineering & Computer Science (AREA)
  • General Chemical & Material Sciences (AREA)
  • Biotechnology (AREA)
  • Biophysics (AREA)
  • Medicinal Chemistry (AREA)
  • Molecular Biology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
DK198902712A 1988-06-06 1989-06-02 Fremgangsmåde til fremstilling af hydroxysyrer DK172667B1 (da)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CH213888 1988-06-06
CH213888 1988-06-06

Publications (3)

Publication Number Publication Date
DK271289D0 DK271289D0 (da) 1989-06-02
DK271289A true DK271289A (da) 1989-12-07
DK172667B1 DK172667B1 (da) 1999-05-10

Family

ID=4226761

Family Applications (1)

Application Number Title Priority Date Filing Date
DK198902712A DK172667B1 (da) 1988-06-06 1989-06-02 Fremgangsmåde til fremstilling af hydroxysyrer

Country Status (14)

Country Link
US (1) US5098841A (da)
EP (1) EP0347374B1 (da)
JP (1) JP2873236B2 (da)
KR (1) KR0165102B1 (da)
AT (1) ATE98697T1 (da)
CA (1) CA1336081C (da)
DE (1) DE58906409D1 (da)
DK (1) DK172667B1 (da)
ES (1) ES2059817T3 (da)
FI (1) FI95047C (da)
IE (1) IE63497B1 (da)
IL (1) IL90527A (da)
MX (1) MX170725B (da)
PT (1) PT90747B (da)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE68926389T2 (de) * 1988-02-08 1996-08-14 Daicel Chem Verfahren zur herstellung optisch aktiver 2-hydroxy-4-phenylbutansäure
US5256552A (en) * 1988-02-08 1993-10-26 Daicel Chemical Industries, Ltd. Process for the production of optically active 2-hydroxy-4-phenylbutyric acid
US5371014A (en) * 1988-02-12 1994-12-06 Daicel Chemical Industries, Ltd. Process for the production of optically active 2-hydroxy acid esters using microbes to reduce the 2-oxo precursor
WO1993013215A1 (en) * 1991-12-23 1993-07-08 Genzyme Limited Synthesis of homochiral 2-hydroxy acids
US5770410A (en) * 1992-01-30 1998-06-23 Genzyme Corporation Chiral synthesis with modified enzymes
GB9413710D0 (en) * 1994-07-07 1994-08-24 Genzyme Ltd Chiral synthesis
RU2278612C2 (ru) * 2000-07-14 2006-06-27 Лайфскен, Инк. Иммуносенсор
EP1326993B1 (en) * 2000-10-17 2007-05-23 Excelsyn Molecular Development Limited Production of alpha-hydroxy-carboxylic acids using a coupled enzyme system
WO2006129320A2 (en) * 2005-06-01 2006-12-07 Yissum Research Development Company Of The Hebrew University Of Jerusalem Biodegradable polymers having a pre-determined chirality
WO2008038300A1 (en) * 2006-09-29 2008-04-03 Council Of Scientific & Industrial Research Organic-inorganic hybrid chiral sorbent and process for the preparation thereof
CN101302503B (zh) * 2007-05-08 2011-04-06 上海医药工业研究院 突变的植物乳杆菌d-乳酸脱氢酶及其基因、重组酶和应用
WO2011009849A2 (en) 2009-07-21 2011-01-27 Basf Se Method for preparing optically active hydroxy acid esters
AU2018227588B2 (en) * 2017-03-03 2021-01-21 Gilead Sciences, Inc. Processes for preparing ACC inhibitors and solid forms thereof
CN109234325A (zh) * 2017-07-11 2019-01-18 上海弈柯莱生物医药科技有限公司 一种乳酸脱氢酶在不对称合成手性羟基化合物中的应用

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CH628009A5 (de) * 1977-07-26 1982-02-15 Hoffmann La Roche Verfahren zur herstellung von optisch aktiven alpha-hydroxycarbonsaeuren.
DE2930087A1 (de) * 1979-07-25 1981-02-26 Biotechnolog Forschung Gmbh Verfahren zur kontinuierlichen enzymatischen umwandlung von wasserloeslichen alpha -ketocarbonsaeuren in die entsprechenden alpha -hydroxycarbonsaeuren
US4785089A (en) * 1985-06-13 1988-11-15 Ciba-Geigy Corporation Novel sulfonic acid esters and their preparation

Also Published As

Publication number Publication date
CA1336081C (en) 1995-06-27
EP0347374A1 (de) 1989-12-20
FI95047B (fi) 1995-08-31
IL90527A0 (en) 1990-01-18
JPH0239893A (ja) 1990-02-08
EP0347374B1 (de) 1993-12-15
IL90527A (en) 1993-05-13
US5098841A (en) 1992-03-24
DK172667B1 (da) 1999-05-10
JP2873236B2 (ja) 1999-03-24
KR0165102B1 (ko) 1999-01-15
IE891821L (en) 1989-12-06
ATE98697T1 (de) 1994-01-15
DE58906409D1 (de) 1994-01-27
FI892702A0 (fi) 1989-06-02
MX170725B (es) 1993-09-09
ES2059817T3 (es) 1994-11-16
IE63497B1 (en) 1995-05-03
PT90747B (pt) 1994-10-31
FI95047C (fi) 1995-12-11
DK271289D0 (da) 1989-06-02
FI892702A (fi) 1989-12-07
KR910001065A (ko) 1991-01-30
PT90747A (pt) 1989-12-29

Similar Documents

Publication Publication Date Title
DK271289A (da) Fremgangsmaade til fremstilling af hydroxysyrer
US4371618A (en) Process for enzymatically producing L-carnitine
AU2829292A (en) Saccharin derivative proteolytic enzyme inhibitors
AU6328094A (en) Saccharin derivative proteolytic enzyme inhibitors
EP0148132B1 (en) Microbiological process for stereoselectively synthesizing l(-)-carnitine
DK0625571T3 (da) Mikroorganismer, deres anvendelse samt fremgangsmåde til fremstilling af L-alfa-aminosyrer
AU2882889A (en) Process for the preparation of optically active 2-arylpropionic acids
Huh et al. Synthesis of l-proline from the racemate by coupling of enzymatic enantiospecific oxidation and chemical non-enantiospecific reducation
DK0574586T3 (da) Fremgangmåde til fremstilling af føde- og drikkevarer
Stoolmiller et al. Formation of α-ketoglutaric semialdehyde from l-2-keto-3-deoxyarabonic acid and isolation of l-2-keto-3-deoxyarabonate dehydratase from Pseudomonas saccharophila
KR0139525B1 (ko) 신규한 에스테라제 및 그의 제조방법
EP0120440A3 (en) Nad(p)-independent glycerol dehydrogenase, process for its preparation and its use in the determination of glycerol and triglycerides
Smeland et al. The 3-hydroxyacyl-CoA epimerase activity of rat liver peroxisomes is due to the combined actions of two enoyl-CoA hydratases: a revision of the epimerase-dependent pathway of unsaturated fatty acid oxidation
AU7072894A (en) Process for the esterification of carboxylic acids with tertiary alcohols
AU5911696A (en) Flavoring agent
Yamasaki et al. δ-Aminolevulinic acid dehydratase of Mycobacterium phlei
MORINO et al. ENZYMATIC STUDIES ON PYRIDOXINE METABOLISM II. A PYRIDOXINE OXIDIZING ENZYME SYSTEM
IE902338L (en) Resolution of pyrrolidone carboxylic acid esters
JPH09224660A (ja) アルデヒド脱水素酵素
KR890003955A (ko) 광학 활성 인-함유 작용성 아세트산 유도체의 효소적 제조방밥
AU548110B2 (en) Process and reagent for the determination of transaminasae
Reeves et al. Function of malate synthetase and isocitritase in the growth of bacteria on two-carbon compounds
Esaki et al. Preparation of stereoselectively-deuterated NADH and NADPH by coupling of glutamate racemase and glutamate dehydrogenase
FI863678A (fi) Foerfarande foer submers odling av pseudomonas aeruginosa-bakteriestammar.
JPS62239990A (ja) 新規リパーゼ

Legal Events

Date Code Title Description
AHS Application shelved for other reasons than non-payment
B1 Patent granted (law 1993)
PUP Patent expired